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The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Finasteride, often used for hair loss, can potentially cause cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

Aromatase gene variation may increase female hair loss risk.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

Vitamin D receptor is crucial for starting hair growth after birth.

Certain microRNAs in the fluid around eggs are linked to Polycystic Ovary Syndrome and may help diagnose it.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Mutations in the KRT85 gene cause hair and nail problems.

A woman with subacute cutaneous lupus erythematosus had widespread skin symptoms triggered by medication and sunlight, which improved with specific treatments.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Mice with enhanced regeneration abilities may help develop new regenerative medicine therapies.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Certain microRNAs are linked to various skin diseases and could be used to diagnose and treat these conditions.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.